HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Cyano-N-[(2S)-2-(3,4-dichlorophenyl)-4-oxobutyl)-N-methyl-1-naphthamide → N-[2-(S)-(3,4-Dichlorophenyl)-4-[4-[2-(methylsulfonyl)-4-methoxyphenyl]-1-piperidinyl]-butyl]-N-methyl-3-cyano-1-naphthamide Hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Cyano-N-[(2S)-2-(3,4-dichlorophenyl)-4-oxobutyl)-N-methyl-1-naphthamide | HCID 18715645 | — |
| Reactant | 4-(2-Methylsulfonyl-4-methoxyphenyl)piperidine | HCID 22622334 | — |
| Product | N-[2-(S)-(3,4-Dichlorophenyl)-4-[4-[2-(methylsulfonyl)-4-methoxyphenyl]-1-piperidinyl]-butyl]-N-methyl-3-cyano-1-naphthamide Hydrochloride | HCID 18715621 | — |
Reaction Steps
Using standard reductive amination conditions N-[2-(S)-(3,4-dichlorophenyl)-4-oxobutyl]-N-methyl-3-cyano-1-naphthamide (0.130 g) was reacted with 4-(2-methylsulfonyl-4-methoxyphenyl)piperidine (0.082 g) and the product (0.074 g) was converted to the hydrochloride salt. MS m/z 678 (M+H). 1H NMR (DMSO-d6) δ 10.57 (m, 1H), 8.62 (m, 1H), 8.10 (m, 1H), 7.95-7.00 (m, 10H), 3.83 (s, 3H), 3.32 (s, 3H), 3.64-1.65 (m, 19H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06365602B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-0252e0cc72e6406c8d3803d75bad39a8 |
| Source note | uspto-grants-2002_04 |